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rs199472726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472726(G;T)
Make rs199472726(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572880
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472726
ebirs199472726
HLIrs199472726
Exacrs199472726
Varsomers199472726
Maprs199472726
PheGenIrs199472726
hapmaprs199472726
1000 genomesrs199472726
hgdprs199472726
ensemblrs199472726
gopubmedrs199472726
geneviewrs199472726
scholarrs199472726
googlers199472726
pharmgkbrs199472726
gwascentralrs199472726
openSNPrs199472726
23andMers199472726
23andMe allrs199472726
SNP Nexus

SNPshotrs199472726
SNPdbers199472726
MSV3drs199472726
GWAS Ctlgrs199472726
Max Magnitude0
ClinVar
Risk rs199472726(A,T;A,T)
Alt rs199472726(A,T;A,T)
Reference rs199472726(G;G)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2594110G>A; NC_000011.9:g.2594110G>T
CLNSRC ClinVar
CLNACC RCV000046134.3, RCV000057767.2, RCV000057768.2,